SHOFU GLASIONOMER FX ULTRA - Indonesia BPOM Medical Device Registration
SHOFU GLASIONOMER FX ULTRA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602818722. The device is manufactured by SHOFU, INC. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MORITA DENTAL INDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHOFU, INC.Country of Origin
Japan
Authorized Representative
MORITA DENTAL INDOAR Address
Ruko Roxy Trade Center Jl. KH. Hasyim Ashari No.233 K Kel.Cideng Kec.Gambir
Registration Date
Feb 27, 2023
Expiry Date
Nov 29, 2027
Product Type
Prosthetic Dental Equipment
Tooth shade resin material.
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